Equilibrating isomers: Bromoindoles and a seco-xanthine encountered during a study of nematocides from the southern Australian marine sponge Hymeniacidon sp.


Autoria(s): Capon, Robert J.; Skene, Colin; Vuong, Dat; Lacey, Ernest; Gill, Jennifer H.; Heiland, Kirstin; Friedel, Thomas
Data(s)

01/01/2002

Resumo

Bioassay-directed fractionation of a Hymeniacidon sp. yielded as nematocidal agents the equilibrating E/Z bromoindole ethyl esters 1 and 2 and corresponding methyl esters 3 and 4. Also isolated for the first time as a natural product was an equilibrating mixture of seco-xanthine formamides, attributed the trivial name hymeniacidin (5). The structure for 5 was assigned on the basis of detailed spectroscopic analysis and total synthesis.

Identificador

http://espace.library.uq.edu.au/view/UQ:38060

Idioma(s)

eng

Publicador

American Chemical Society

Palavras-Chave #Plant Sciences #Chemistry, Applied #Chemistry, Medicinal #Pharmacology & Pharmacy #Metabolites #030401 Biologically Active Molecules #030502 Natural Products Chemistry
Tipo

Journal Article